16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study-Reference-Cited by-同舟云学术

16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

Published:2006-09 Issue:2 Volume:247 Page:180-186
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Ouyang Y.,Sakoe K.,Shimazaki H.,Namekawa M.,Ogawa T.,Ando Y.,Kawakami T.,Kaneko J.,Hasegawa Y.,Yoshizawa K.,Amino T.,Ishikawa K.,Mizusawa H.,Nakano I.,Takiyama Y.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference26 articles.

1. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias: a study of 11 families, including descendants of “Drew family of Walworth”;Harding;Brain,1982

2. The wide spectrum of spinocerebellar ataxias (SCAs);Manto;Cerebellum,2005

3. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2;Cagnoli;Brain,2006

4. Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1;Flanigan;Am J Hum Genet,1996

5. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region;Hellenbroich;J Neurol,2003

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